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DNA methylation studies on imprinted loci in a male monozygotic twin pair discordant for Beckwith-Wiedemann syndrome.

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In vitro evaluation of the cytotoxic and mutagenic potential of the 5-aminolevulinic acid hexylester-mediated photodynamic therapy.

Mutation research·2004

High rate of constitutional chromosomal rearrangements in apparently sporadic ALS.

Neurology·2003

Mutagenic and cytotoxic effectiveness of diisopropyl xanthogen polysulphide in human lymphocyte cultures.

Mutation research·2003

Frequent mitotic errors in tumor cells of genetically micro-heterogeneous glioblastomas.

Cytogenetics and cell genetics·2001

Predictive value of progression-associated chromosomal aberrations for the prognosis of meningiomas: a retrospective study of 198 cases.

Journal of neurosurgery·2001

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Humangenetik·1975

Climate associated variations in the human serum albumin level.

Humangenetik·1975

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Humangenetik·1975

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Humangenetik·1975

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

Humangenetik·1975

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

Humangenetik·1975

Overcoming a diagnostic blindspot: Identifying balanced translocations in Mendelian rare disease cohorts.

medRxiv : the preprint server for health sciences·2026

Organelle Volume Facilitates Spindle Positioning During C . elegans Female Meiosis.

bioRxiv : the preprint server for biology·2026

Somatic instability of the C9orf72 repeat expansion in blood differs between patients with amyotrophic lateral sclerosis or frontotemporal dementia.

medRxiv : the preprint server for health sciences·2026

FAT1 generates a nuclear fragment that impairs DNA damage repair in gastric cancer.

The Journal of biological chemistry·2026

Results from the VANISH study: A prospective multicenter study validating a single-nucleotide polymorphism-based noninvasive prenatal test to assess aneuploidy risk in surviving twins of vanishing twin pregnancies.

Pregnancy (Hoboken, N.J.)·2026

Loss-of-function variants in CFAP57, SEPTIN4, SPEM2, and CFAP46 cause asthenoteratozoospermia.

Human reproduction (Oxford, England)·2026

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Cytological and cytogenetical studies on brain tumors. 3. Ph1-like chromosomes in human meningiomas

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DNA methylation studies on imprinted loci in a male monozygotic twin pair discordant for Beckwith-Wiedemann syndrome.

In vitro evaluation of the cytotoxic and mutagenic potential of the 5-aminolevulinic acid hexylester-mediated photodynamic therapy.

High rate of constitutional chromosomal rearrangements in apparently sporadic ALS.

Mutagenic and cytotoxic effectiveness of diisopropyl xanthogen polysulphide in human lymphocyte cultures.

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